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1.
Coral proxy records of sea surface temperature (SST) and hydrological balance have become important tools in the field of tropical paleoclimatology. However, coral aragonite is subject to post-depositional diagenetic alteration in both the marine and vadose environments. To understand the impact of diagenesis on coral climate proxies, two mid-Holocene Porites corals from raised reefs on Muschu Island, Papua New Guinea, were analysed for Sr/Ca, δ18O, and δ13C along transects from 100% aragonite to 100% calcite. Thin-section analysis showed a characteristic vadose zone diagenetic sequence, beginning with leaching of primary aragonite and fine calcite overgrowths, transitional to calcite void filling and neomorphic, fabric selective replacement of the coral skeleton. Average calcite Sr/Ca and δ18O values were lower than those for coral aragonite, decreasing from 0.0088 to 0.0021 and −5.2 to −8.1‰, respectively. The relatively low Sr/Ca of the secondary calcite reflects the Sr/Ca of dissolving phases and the large difference between aragonite and calcite Sr/Ca partition coefficients. The decrease in δ18O of calcite relative to coral aragonite is a function of the δ18O of precipitation. Carbon-isotope ratios in secondary calcite are variable, though generally lower relative to aragonite, ranging from −2.5 to −10.4%. The variability of δ13C in secondary calcite reflects the amount of soil CO2 contributing 13C-depleted carbon to the precipitating fluids. Diagenesis has a greater impact on Sr/Ca than on δ18O; the calcite compositions reported here convert to SST anomalies of 115°C and 14°C, respectively. Based on calcite Sr/Ca compositions in this study and in the literature, the sensitivity of coral Sr/Ca-SST to vadose-zone calcite diagenesis is 1.1 to 1.5°C per percent calcite. In contrast, the rate of change in coral δ18O-SST is relatively small (−0.2 to 0.2°C per percent calcite). We show that large shifts in δ18O, reported for mid-Holocene and Last Interglacial corals with warmer than present Sr/Ca-SSTs, cannot be caused by calcite diagenesis. Low-level calcite diagenesis can be detected through X-ray diffraction techniques, thin section analysis, and high spatial resolution sampling of the coral skeleton and thus should not impede the production of accurate coral paleoclimate reconstructions.  相似文献   

2.
The integrity of coral-based reconstructions of past climate variability depends on a comprehensive knowledge of the effects of post-depositional alteration on coral skeletal geochemistry. Here we combine millimeter-scale and micro-scale coral Sr/Ca data, scanning electron microscopy (SEM) images, and X-ray diffraction with previously published δ18O records to investigate the effects of submarine and subaerial diagenesis on paleoclimate reconstructions in modern and young sub-fossil corals from the central tropical Pacific. In a 40-year-old modern coral, we find secondary aragonite is associated with relatively high coral δ18O and Sr/Ca, equivalent to sea-surface temperature (SST) artifacts as large as −3 and −5 °C, respectively. Secondary aragonite observed in a 350-year-old fossil coral is associated with relatively high δ18O and Sr/Ca, resulting in apparent paleo-SST offsets of up to −2 and −4 °C, respectively. Secondary Ion Mass Spectrometry (SIMS) analyses of secondary aragonite yield Sr/Ca ratios ranging from 10.78 to 12.39 mmol/mol, significantly higher compared to 9.15 ± 0.37 mmol/mol measured in more pristine sections of the same fossil coral. Widespread dissolution and secondary calcite observed in a 750-year-old fossil coral is associated with relatively low δ18O and Sr/Ca. SIMS Sr/Ca measurements of the secondary calcite (1.96-9.74 mmol/mol) are significantly lower and more variable than Sr/Ca values from more pristine portions of the same fossil coral (8.22 ± 0.13 mmol/mol). Our results indicate that while diagenesis has a much larger impact on Sr/Ca-based paleoclimate reconstructions than δ18O-based reconstructions at our site, SIMS analyses of relatively pristine skeletal elements in an altered coral may provide robust estimates of Sr/Ca which can be used to derive paleo-SSTs.  相似文献   

3.
Chemical proxies are useful analogs for reconstructing physical properties of sea water, such as sea surface temperature (SST) and sea surface salinity (SSS). Time series of these inferred properties would allow for reconstructions of past El Niño–Southern Oscillation (ENSO) events, where no instrumental records exist. In this study, a monthly oxygen isotope record from a Porites coral is used to explain how past ENSO events are recorded in the coral skeletons. The sample covers a 12 year period and was collected from Nanwan Bay, Taiwan. During El Niño events the coral skeleton is shown to produce a δ18O–SST correlation with a slope of −0.12 ± 0.04‰ °C−1. During other times, this value is significantly different, with a slope of −0.21 ± 0.04‰ °C−1. Coral that grew during El Niño summers have δ18O values which are enriched by ∼0.2‰, relative to other times. A possible mechanism to explain this difference may be enhanced penetration of Kuroshio Current waters into the South China Sea during summer. The observed contrast in the correlation of δ18O–SST variability in this sample supports the influence of El Niño in eastern Asia.  相似文献   

4.
The geochemistry of coral skeletons may reflect seawater conditions at the time of deposition and the analysis of fossil skeletons offers a method to reconstruct past climate. However the precipitation of cements in the primary coral skeleton during diagenesis may significantly affect bulk skeletal geochemistry. We used secondary ion mass spectrometry (SIMS) to measure Sr, Mg, B, U and Ba concentrations in primary coral aragonite and aragonite and calcite cements in fossil Porites corals from submerged reefs around the Hawaiian Islands. Cement and primary coral geochemistry were significantly different in all corals. We estimate the effects of cement inclusion on climate estimates from drilled coral samples, which combine cements and primary coral aragonite. Secondary 1% calcite or ∼2% aragonite cement contamination significantly affects Sr/Ca SST estimates by +1 °C and −0.4 to −0.9 °C, respectively. Cement inclusion also significantly affects Mg/Ca, B/Ca and U/Ca SST estimates in some corals. X-ray diffraction (XRD) will not detect secondary aragonite cements and significant calcite contamination may be below the limit of detection (∼1%) of the technique. Thorough petrographic examination of fossils is therefore essential to confirm that they are pristine before bulk drilled samples are analysed. To confirm that the geochemistry of the original coral structures is not affected by the precipitation of cements in adjacent pore spaces we analysed the primary coral aragonite in cemented and uncemented areas of the skeleton. Sr/Ca, B/Ca and U/Ca of primary coral aragonite is not affected by the presence of cements in adjacent interskeletal pore spaces i.e. the coral structures maintain their original composition and selective SIMS analysis of these structures offers a route to the reconstruction of accurate SSTs from altered coral skeletons. However, Mg/Ca and Ba/Ca of primary coral aragonite are significantly higher in parts of skeletons infilled with high Mg calcite cement. We hypothesise this reflects cement infilling of intraskeletal pore spaces in the primary coral structure.  相似文献   

5.
To understand Holocene climate evolutions in low-latitude region of the western Pacific, paired δ18O and Mg/Ca records of planktonic foraminifer Globigerinoides ruber (250–300 μm, sensu stricto, s.s.) from a marine core ORI715-21 (121.5°E, 22.7°N, water depth 760 m) underneath the Kuroshio Current (KC) off eastern Taiwan were analyzed. Over the past 7500 years, the geochemical proxy-inferred sea surface temperature (SST) hovered around 27–28 °C and seawater δ18O (δ18OW) slowly decreased 0.2–0.4‰ for two KC sites at 22.7° and 25.3°N. Comparison with a published high-SST and high-salinity equatorial tropical Pacific record, MD98-2181 located at the Mindanao Current (MC) at 6.3°N, reveals an anomalous time interval at 3.5–1.5 kyr ago (before 1950 AD). SST gradient between the MC site and two KC site decrease from 1.5–2.0 °C to only 0–1 °C, and δ18OW from 0.1–0.3‰ to 0‰ for this 2-kyr time window. The high SST and low gradient could result from a northward shift of the North Equatorial Current, which implies a weakened KC. The long-term descending δ18OW and increasing precipitation in the entire low-latitude western Pacific and the gradually decreasing East Asian summer monsoonal rainfall during middle-to-late Holocene is likely caused by different land and ocean responses to solar insolation and/or enhanced moisture transportation from the Atlantic to Pacific associated with the southward movement of ITCZ.  相似文献   

6.
《Chemical Geology》2007,236(3-4):339-349
We present a new high precision analytical method for the determination of Mg/Ca and Sr/Ca ratios in carbonates using an inductively coupled plasma quadrupole mass spectrometer (ICP-QMS) with a 650-W cold plasma technique and a desolvation introduction system. Signal intensities are detected in pulse-counting mode and Mg/Ca and Sr/Ca ratios are calculated directly from intensity ratios of 24Mg/43Ca and 86Sr/43Ca using external matrix-matched standards for every 4–5 samples to correct for instrumental mass discrimination and low-frequency ratio drift. Significant matrix effect of Ca content on Mg/Ca determination (− 0.018 Mg/Ca (mmol/mol)/[Ca] (ppm)), can be overcome by diluting [Ca] to 6–8 ppm in the sample solution or using an empirical correction. The Sr/Ca ratio affects the Mg/Ca determination, with a factor of − 0.32% Mg/Ca per mmol/mol. This is mainly caused by the influence of doubly charged 86Sr, which biases the intensity measurement of the 43Ca+ ion beam. This effect results in a trivial offset of less than 0.1% on Mg/Ca measurements for Quaternary foraminiferal and coral samples. The internal precision of our method ranges from 0.1 to 0.2%. Replicate measurements made on standards and samples show long-term external uncertainties (2σ) of Mg/Ca = 0.84% and Sr/Ca = 0.49%. The minimum sample size requirement is only 3.5 μg of carbonate. The application of this newly developed technique on the planktonic foraminifera Globigerinoides ruber from a core recovered in the southern South China Sea yields a glacial–interglacial difference in sea surface temperature (SST) of 3 °C. Three-year coral Sr/Ca data suggest that the seasonal SST ranged from 22.6–23.8 °C in winter to 26.9–27.9 °C in summer in Nanwan, south Taiwan, during 2000–2002. The coral-Sr/Ca inferred SSTs in 2002 match well with instrumental records, which demonstrates the validity of this ICP-QMS method.  相似文献   

7.
Hydrography of the Bay of Bengal is highly influenced by the river runoff and rainfall during the southwest monsoon. We have reconstructed δ18Osw, sea surface salinity and sea surface temperature (SST) changes in the Bay of Bengal by using paired measurements of δ18O and Mg/Ca in a planktonic foraminifera species Globigerinoides ruber from core SK218/1 in the western Bay of Bengal in order to understand the rainfall variability associated with southwest monsoon over the past 32 kyr. Our SST reconstructions reveal that Bay of Bengal was ～3.2 °C cooler during the LGM as compared to present day temperature and a ～3.5 °C rise in SST is documented from 17 to 10 ka. Both SST and δ18Osw exhibit greater amplitude fluctuations during MIS 2 which is attributable to the variability of NE monsoon rainfall and associated river discharge into the Bay of Bengal in association with strong seasonal temperature contrast. On set of strengthening phase of SW monsoon was started during Bølling/Allerød as evidenced by the low δ18Osw values ～14.7 ka. δ18Osw show consistently lower values during Holocene (with an exception around 5 ka), which suggests that the freshening of Bay of Bengal due to heavy precipitation and river discharge caused by strong SW monsoon. Results of this study signify that the maximum fluctuations of the NE monsoon rainfall during MIS 2 appear to be controlled by the strong seasonality and boundary conditions.  相似文献   

8.
The isotopic composition of water and dissolved Sr as well as other geochemical parameters at the 2516 m deep Outokumpu Deep Drill Hole, Finland were determined. The drill hole is hosted by Palaeoproterozoic turbiditic metasediments, ophiolite-derived altered ultramafic rocks and pegmatitic granitoids. Sodium–Ca–Cl and Ca–Na–Cl-rich waters (total dissolved solids up to ca. 70 g L−1) containing significant amounts of gas, mainly CH4 (up to 32 mmol L−1), N2 (up to 10 mmol L−1), H2 (up to 3.1 mmol L−1) and He (up to 1.1 mmol L−1) discharge from fracture zones into the drill hole. This water is distinct from the shallow fresh groundwater of the area, and has an isotopic composition typical of shield brines that have been modified during long-term water–rock interaction. Based on water stable isotopes and geochemistry, the drill hole water profile can be divided into five water types, each discharging from separate fracture systems and affected by the surrounding rocks. The δ2H varies from −90‰ to −56‰ (VSMOW) and δ18O from −13.5‰ to −10.4‰ (VSMOW), plotting clearly above the Global and Local Meteoric Water Lines on a δ2H vs. δ18O diagram. The 87Sr/86Sr ratios range between 0.72423 and 0.73668. Simple two-component mixing between 2H and 18O rich end-member brine and meteoric water cannot explain the water stable isotopic composition and trends observed. Instead, hydration of silicates by ancient groundwaters recharged under different climatic conditions, warmer than at present, is the most likely mechanism to have caused the variation of the δ2H and δ18O values. Water types correlate with changes in microbial communities implying that different ecosystems occur at different depths. The different water types and microbial populations have remained isolated from each other and from the surface for long periods of time, probably tens of millions of years.  相似文献   

9.
To reconstruct oceanographic variations in the subtropical South Pacific, 271-year long subseasonal time series of Sr/Ca and δ18O were generated from a coral growing at Rarotonga (21.5°S, 159.5°W). In this case, coral Sr/Ca appears to be an excellent proxy for sea surface temperature (SST) and coral δ18O is a function of both SST and seawater δ18O composition (δ18Osw). Here, we focus on extracting the δ18Osw signal from these proxy records. A method is presented assuming that coral Sr/Ca is solely a function of SST and that coral δ18O is a function of both SST and δ18Osw. This method separates the effects of δ18Osw from SST by breaking the instantaneous changes of coral δ18O into separate contributions by instantaneous SST and δ18Osw changes, respectively. The results show that on average δ18Osw at Rarotonga explains ∼39% of the variance in δ18O and that variations in SST explains the remaining ∼61% of δ18O variance. Reconstructed δ18Osw shows systematic increases in summer months (December-February) consistent with the regional pattern of variations in precipitation and evaporation. The δ18Osw also shows a positive linear correlation with satellite-derived estimated salinity for the period 1980 to 1997 (r = 0.72). This linear correlation between reconstructed δ18Osw and salinity makes it possible to use the reconstructed δ18Osw to estimate the past interannual and decadal salinity changes in this region. Comparisons of coral δ18O and δ18Osw at Rarotonga with the Pacific decadal oscillation index suggest that the decadal and interdecadal salinity and SST variability at Rarotonga appears to be related to basin-scale decadal variability in the Pacific.  相似文献   

10.
With an aim to increase the understanding about the isotopic and chemical heterogeneity of calcites in water-conducting fracture zones with different crystalline wall rock compositions at different depths, we present trace element chemistry, isotopic composition (δ18O, δ13C, 87Sr/86Sr) and biomarkers of euhedral low-temperature fracture-coating calcite. Paleohydrogeological fluctuations and wall rock influence on the hydrochemistry in the deep groundwater are explored. Samples are from several fracture zone sub-fractures (at −360 to −740 m), retrieved during an extensive core drilling campaign in Sweden.Calcite generally showed fracture zone specific values of δ13C, δ18O and 87Sr/86Sr, which indicates precipitation from relatively homogeneous fluid (similar to the modern groundwater at the site) at the same event in each fracture zone. δ18O and δ13C in the different fracture zones were consistent with precipitation from waters of different salinity and decreasing organic input with depth, respectively. The latter is also supported by biomarkers showing clear indications of SRB-related organic compounds (e.g. iso- and anteiso-C17:0-branched fatty acids), except in the deepest zone. In contrast to the isotopes, variation in trace elements within the fracture zones was generally up to several orders of magnitude. Manganese and REE, as oppose to the other metals, were higher in the shallow fracture zones (112–1130 and 44–97 ppm, respectively) than in the deeper (28–272 and 5–11 ppm, respectively), in agreement with the groundwater composition. Although the rock types varied between and within the different fracture zones, this had insignificant influence on the trace element chemistry of the calcites. Co-variation was generally relatively large for many trace elements, with isometric logratio correlation generally better than 0.75, which indicates that their variation in the calcites is due to variation of Ca in the fracture water, but other local factors, especially uptake in co-precipitating minerals (clay minerals, barite, pyrite and zeolites), but also microbial activity and metal speciation may have influenced the metal incorporation into calcite. These detailed studies of fracture calcite are of importance for the understanding of variation in fluid chemistry and trace metal uptake in fracture zones, adding together with hydrochemical studies detailed information optimal for site characterisation.  相似文献   

11.
《Quaternary Science Reviews》2007,26(19-21):2586-2597
Recent paleoclimatic work on terrestrial and marine deposits from Asia and the Indian Ocean has indicated abrupt changes in the strength of the Asian monsoon during the last deglaciation. Comparison of marine paleoclimate records that track salinity changes from Asian rivers can help evaluate the coherence of the Indian Ocean monsoon (IOM) with the larger Asian monsoon. Here we present paired Mg/Ca and δ18O data on the planktic foraminifer Globigerinoides ruber (white) from Andaman Sea core RC12-344 that provide records of sea-surface temperature (SST) and δ18O of seawater (δ18Osw) over the past 25,000 years (ka) before present (BP). Age control is based on nine accelerator mass spectrometry (AMS) dates on mixed planktic foraminifera. Mg/Ca-SST data indicate that SST was ∼3 °C cooler during the last glacial maximum (LGM) than the late Holocene. Andaman Sea δ18Osw exhibited higher than present values during the Lateglacial interval ca 19–15 ka BP and briefly during the Younger Dryas ca 12 ka BP. Lower than present δ18Osw values during the BØlling/AllerØd ca 14.5–12.6 ka BP and during the early Holocene ca 10.8–5.5 ka BP are interpreted to indicate lower salinity, reflect some combination of decreased evaporation–precipitation (E–P) over the Andaman Sea and increased Irrawaddy River outflow. Our results are consistent with the suggestion that IOM intensity was stronger than present during the BØlling/AllerØd and early Holocene, and weaker during the late glaciation, Younger Dryas, and the late Holocene. These findings support the hypothesis that rapid climate change during the last deglaciation and Holocene included substantial hydrologic changes in the IOM system that were coherent with the larger Asian monsoon.  相似文献   

12.
The Yangla Cu deposit is the largest Cu skarn deposit in the Jinshajiang tectonic belt. Based on the detailed observation of crosscutting relationships, three mineralization stages (i.e., pre-ore, ore and supergene) have been identified in the Yangla deposit. The pre-ore stage is dominated by prograde skarn. The ore stage is characterized by the precipitation of hydrous silicate minerals, Fe-oxides, Fe-Cu-Mo-sulfides, quartz and calcite, whose mineral assemblages were formed in the early and late sub-ore stages. The early sub-ore stage is marked by retrograde alteration with the deposition of hydrous silicate minerals (e.g., actinolite, epidote and chlorite), Fe-oxides, abundant Fe-Cu-Mo-sulfides, quartz and minor calcite. Whilst, the late sub-ore stage, associated with silicic and carbonate alteration, is represented by widespread thick quartz or calcite veins with disseminated pyrite, chalcopyrite, galena and sphalerite. We present new carbon-oxygen (C-O) isotopic compositions of the ore-hosting marble and hydrothermal calcite of this deposit. The hydrothermal calcite in the Yangla deposit was precipitated from both the early and late sub-ore stages. Calcite I from the early sub-ore stage is anhedral, and occurs as spot in the skarn or locally replaces the skarn minerals. Calcite II from the late sub-ore stage is distinguished by being coarse-grained, subhedral to euhedral and its occurrence in thick veins. Calcite I contains lower δ13CPDB (−7.0‰ to −5.0‰) and δ18OSMOW (7.2‰ to 12.7‰) than Calcite II (δ13CPDB = −4.5‰ to −2.3‰; δ18OSMOW = 10.7‰ to 19.4‰). In the δ13CPDB vs. δ18OSMOW diagram, the Calcite I and Calcite II data fall close to the igneous carbonatite field and between the fields of igneous carbonatite and marine carbonates, respectively. This suggests a dominantly magmatic origin for the early sub-ore fluids, and there might have been increasing carbonate wall rock involvement towards the late sub-ore stage. The ore-hosting marble (δ13CPDB = −4.8‰ to −0.3‰; δ18OSMOW = 10.2‰ to 23.9‰) also shows a positive δ13CPDB vs. δ18OSMOW correlation, which is interpreted to reflect the decreasing alteration intensity during the interactions between the hydrothermal fluids and ore-hosting carbonates. Simulated calculation suggests that both the Calcite I and Calcite II precipitated at 350 °C to 250 °C and 250 °C to 150 °C, respectively. We proposed that CO2 degassing and water/rock interactions were likely the two major processes that precipitated the calcite and led to the observed C-O isotopic features of the Yangla Cu deposit.  相似文献   

13.
The Diyadin Geothermal area, located in the eastern part of Anatolia (Turkey) where there has been recent volcanic activity, is favorable for the formation of geothermal systems. Indeed, the Diyadin geothermal system is located in an active geodynamic zone, where strike-slip faults and tensional cracks have developed due to N–S regional compression. The area is characterized by closely spaced thermal and mineralized springs, with temperatures in the range 30–64 °C, and flowrates 0.5–10 L/s. Thermal spring waters are mainly of Ca(Na)-HCO3 and Ca(Mg)-SO4 types, with high salinity, while cold groundwater is mostly of Ca(Na, Mg)-HCO3 type, with lower salinity. High contents of some minor elements in thermal waters, such as F, B, Li, Rb, Sr and Cs probably derive from enhanced water–rock interaction.Thermal water samples collected from Diyadin are far from chemical equilibrium as the waters flow upward from reservoirs towards spring vents and possibly mix with cooler waters. The temperatures of the deep geothermal reservoirs are estimated to be between 92 and 156 °C in Diyadin field, based on quartz geothermometry, while slightly lower estimates are obtained using chalcedony geothermometers. The isotopic composition of thermal water (δ18O, δ2H, δ3H) indicates their deep-circulating meteoric origin. The waters are likely to have originated from the percolation of rainwater along fractures and faults to the deep hot reservoir. Subsequent heating by conduction due to the presence of an intrusive cupola associated with the Tendurek volcano, is followed by the ascent of deep waters to the surface along faults and fractures that act as hydrothermal conduits.Modeling of the geothermal fluids indicates that the fluid is oversaturated with calcite, aragonite and dolomite, which matches travertine precipitation in the discharge area. Likewise, the fluid is oversaturated with respect to quartz, and chalcedony indicating the possibility of siliceous precipitation near the discharge areas. A conceptual hydro-geochemical model of the Diyadin thermal waters based on the isotope and chemical analytical results, has been constructed.  相似文献   

14.
This study was conducted on recent desert samples—including (1) soils, (2) plants, (3) the shell, and (4) organic matter from modern specimens of the land snail Eremina desertorum—which were collected at several altitudes (316–360 m above sea level) from a site in the New Cairo Petrified Forest. The soils and shellE. desertorum were analyzed for carbonate composition and isotopic composition (δ18O, δ13C). The plants and organic matterE. desertorum were analyzed for organic carbon content and δ13C. The soil carbonate, consisting of calcite plus minor dolomite, has δ18O values from −3.19 to −1.78‰ and δ13C values −1.79 to −0.27‰; covariance between the two values accords with arid climatic conditions. The local plants include C3 and C4 types, with the latter being dominant. Each type has distinctive bulk organic carbon δ13C values: −26.51 to −25.36‰ for C3-type, and −13.74 to −12.43‰ for C4-type plants.The carbonate of the shellE. desertorum is composed of aragonite plus minor calcite, with relatively homogenous isotopic compositions (δ18Omean = −0.28 ± 0.22‰; δ13Cmean = −4.46 ± 0.58‰). Most of the δ18O values (based on a model for oxygen isotope fractionation in an aragonite-water system) are consistent with evaporated water signatures. The organic matterE. desertorum varies only slightly in bulk organic carbon δ13C values (−21.78 ± 1.20‰) and these values suggest that the snail consumed more of C3-type than C4-type plants. The overall offset in δ13C values (−17.32‰) observed between shellE. desertorum carbonate and organic matterE. desertorum exceeds the value expected for vegetation input, and implies that 30% of carbon in the shellE. desertorum carbonate comes from the consumption of limestone material.  相似文献   

15.
This study provides 87Sr/86Sr, δ13C and δ18O data from the best-preserved limestone and dolomite of the Ediacaran carbonate-dominated Khorbusuonka Group of the Olenek Uplift, NE Siberian Craton, as well as detrital zircon geochronological data from both underlying and overlying sandstones. The Maastakh Formation is characterized by 87Sr/86Sr ratios of ca. 0.70822 and δ13C values between + 4.8 and + 6.0‰. 87Sr/86Sr ratios in limestones of the Khatyspyt Formation are fairly uniform, ranging from 0.70783 to 0.70806. The carbon isotopic composition slowly decreases from bottom (+ 3.7‰) to top (− 0.2‰) of section. The Sr isotopic composition of the Turkut Formation varies from 0.70824 to 0.70914, value of δ13C is about zero: − 0.7…+0.7 ‰. The youngest population of detrital zircons from Maastakh Formation indicates that these rocks were formed not later than 630 Ma. U–Pb detrital zircons data of Kessyusa Group has a single peak at about 543 Ma, which is almost identical to the earlier dating. Based on biostratigraphy and isotopic data, the Sr isotopic compositions from the Khatyspyt Formation (87Sr/86Sr = 0.70783–0.70806) represent the composition of seawater at 560–550 Ma. Such low values of 87Sr/86Sr ratio in Ediacaran water were probably caused by the quick opening of Iapetus Ocean.  相似文献   

16.
The Bear Lodge alkaline complex in northeastern Wyoming (USA) is host to potentially economic rare-earth mineralization in carbonatite and carbonatite-related veins and dikes that intrude heterolithic diatreme breccias in the Bull Hill area of the Bear Lodge Mountains. The deposit is zoned and consists of pervasively oxidized material at and near the surface, which passes through a thin transitional zone at a depth of ~ 120–183 m, and grades into unaltered carbonatites at depths greater than ~ 183–190 m. Carbonatites in the unoxidized zone consist of coarse and fine-grained calcite that is Sr-, Mn- and inclusion-rich and are characterized by the presence of primary burbankite, early-stage parisite and synchysite with minor bastnäsite that have high (La/Nd)cn and (La/Ce)cn values. The early minerals are replaced with polycrystalline pseudomorphs consisting of secondary rare-earth fluorocarbonates and ancylite with minor monazite. Different secondary parageneses can be distinguished on the basis of the relative abundances and composition of individual minerals. Variations in key element ratios, such as (La/Nd)cn, and chondrite-normalized profiles of the rare-earth minerals and calcite record multiple stages of hydrothermal deposition involving fluids of different chemistry. A single sample of primary calcite shows mantle-like δ18OV-SMOW and δ13CV-PDB values, whereas most other samples are somewhat depleted in 13C (δ13CV-PDB ≈ − 8 to − 10‰) and show a small positive shift in δ18OV-SMOW due to degassing and wall-rock interaction. Isotopic re-equilibration is more pronounced in the transitional and oxidized zones; large shifts in δ18OV-SMOW (to ~ 18‰) reflect the input of meteoric water during pervasive hydrothermal reworking and supergene oxidation. The textural relations, mineral chemistry and C and O stable-isotopic variations record a polygenetic sequence of rare-earth mineralization in the deposit. With the exception of one Pb-poor sample showing an appreciable positive shift in 208Pb/204Pb value (~ 39.2), the Bear Lodge carbonatites are remarkably uniform in their Nd, Sr and Pb isotopic composition: 143Nd/144Ndt = 0.512591–0.512608; εNdt = 0.2–0.6; 87Sr/86Srt = 0.704555–0.704639; εSrt = − 1.5–2.7; 206Pb/204Pbt = 18.071–18.320; 207Pb/204Pbt = 15.543–15.593; and 208Pb/204Pbt = 38.045–39.165. These isotopic characteristics indicate that the source of the carbonatitic magma was in the subcontinental lithospheric mantle, and modified by subduction-related metasomatism. Carbonatites are interpreted to be generated from small degrees of partial melt that may have been produced via interaction of upwelling asthenosphere giving a small depleted MORB component, with an EM1 component likely derived from subducted Farallon crust.  相似文献   

17.
The Qianfanling Mo deposit, located in Songxian County, western Henan province, China, is one of the newly discovered quartz-vein type Mo deposits in the East Qinling–Dabie orogenic belt. The deposit consists of molybdenite in quartz veins and disseminated molybdenite in the wall rocks. The alteration types of the wall rocks include silicification, K-feldspar alteration, pyritization, carbonatization, sericitization, epidotization and chloritization. On the basis of field evidence and petrographic analysis, three stages of hydrothermal mineralization could be distinguished: (1) pyrite–barite–quartz stage; (2) molybdenite–quartz stage; (3) quartz–calcite stage.Two types of fluid inclusions, including CO2-bearing fluid inclusions and water-rich fluid inclusions, have been recognized in quartz. Homogenization temperatures of fluid inclusions vary from 133 °C to 397 °C. Salinity ranges from 1.57 to 31.61 wt.% NaCl eq. There are a large number of daughter mineral-CO2-bearing inclusions, which is the result of fluid immiscibility. The ore-forming fluids are medium–high temperature, low to moderate salinity H2O–NaCl–CO2 system. The δ34S values of pyrite, molybdenite, and barite range from − 9.3‰ to − 7.3‰, − 9.7‰ to − 7.3‰ and 5.9‰ to 6.8‰, respectively. The δ18O values of quartz range from 9.8‰ to 11.1‰, with corresponding δ18Ofluid values of 1.3‰ to 4.3‰, and δ18D values of fluid inclusions of between − 81‰ and − 64‰. The δ13CV-PDB values of fluid inclusions in quartz and calcite have ranges of − 6.7‰ to − 2.9‰ and − 5.7‰ to − 1.8‰, respectively. Sulfur, hydrogen, oxygen and carbon isotope compositions show that the sulfur and ore-forming fluids derived from a deep-seated igneous source. During the peak collisional period between the North China Craton and the Yangtze Craton, the ore-forming fluids that derived from a deep igneous source extracted base and precious metals and flowed upwards through the channels that formed during tectonism. Fluid immiscibility and volatile exsolution led to the crystallization of molybdenite and other minerals, and the formation of economic orebodies in the Qianfanling Mo deposit.  相似文献   

18.
The magnetite deposits of the Turgai belt (Kachar, Sarbai and Sokolov), in the Valerianovskoe zone of the southern Urals, Kazakhstan, contain a combined resource of over 3 Gt of iron oxide ore. The deposits are hosted by carbonate sediments and volcaniclastic rocks of the Carboniferous Valerianovka Supergroup, and are spatially related to the gabbroic to granitoid composition intrusive rocks of the Sarbai–Sokolov intrusive series. The magnetite deposits are developed dominantly as metasomatic replacement of limestone, but also, to a lesser extent, of volcanic rocks. Pre-mineralisation metamorphism and alteration resulted in the formation of wollastonite and the silicification of limestone. Magnetite mineralisation is associated with the development of a high temperature skarn assemblage of diopside, grossular–andradite garnet, actinolite, epidote and apatite. Sub-economic copper-bearing sulphide mineralisation overprints the magnetite mineralisation and is associated with deposition of hydrothermal calcite and the formation of an extensive sodium alteration halo dominated by albite and scapolite. Chlorite formation accompanies this stage and further later stage hydrothermal overprints. The replacement has in places resulted in preservation of primary features of the limestone, including fossils and sedimentary structures in magnetite, skarn calc-silicates and sulphides.Analysis of Re–Os isotopes in molybdenite indicates formation of the sulphide mineral assemblage at 336.2 ± 1.3 Ma, whilst U–Pb analyses of titanite from the skarn alteration assemblage suggests skarn alteration at 326.6 ± 4.5 Ma with re-equilibration of isotope systematics down to ~ 270 Ma. Analyses of mineral assemblages, fluid inclusion microthermometry, O and S isotopes suggest initial mineralisation temperatures in excess of 600 °C from hypersaline brines (45–50 wt.% NaCl eq.), with subsequent cooling and dilution of fluids to around 150 °C and 20 wt.% NaCl eq. by the time of calcite deposition in late stage sulphide-bearing veins. δ18O in magnetite (− 1.5 to + 3.5‰) and skarn forming silicates (+ 5 to + 9‰), δ18O and δ13C in limestone and skarn calcite (δ18O + 5.4 to + 26.2‰; δ13C − 12.1 to + 0.9‰) and δ34S in sulphides (− 3.3 to + 6.6‰) and sulphates (+ 4.9 to + 12.9‰) are all consistent with the interaction of a magmatic-equilibrated fluid with limestone, and a dominantly magmatic source for S. All these data imply skarn formation and mineralisation in a magmatic–hydrothermal system that maintained high salinity to relatively late stages resulting in the formation of the large Na-alteration halo. Despite the reported presence of evaporites in the area there is no evidence for evaporitic sulphur in the mineralising system.These skarns show similarities to some members of the iron oxide–apatite and iron oxide–copper gold deposit classes and the model presented here may have implications for their genesis. The similarity in age between the Turgai deposits and the deposits of the Magnitogorsk zone in the western Urals suggests that they may be linked to similar magmatism, developed during post-orogenic collapse and extension following the continent–continent collision, which has resulted in the assembly of Laurussian terranes with the Uralide orogen and the Kazakh collage of the Altaids or Central Asian Orogenic Belt. This model is preferred to the model of simultaneous formation of very similar deposits in arc settings at either side of an open tract of oceanic crust forming part of the Uralian ocean.  相似文献   

19.
In the Eastern Dharwar craton, among the many shear zone-hosted lode gold deposits, those at Ramagiri and Penakacherla are located near the western margin of the craton. Mineralized quartz (± sulfide ± carbonate) veins are hosted by the schistose (metavolcanic and carbonaceous metasedimentary) rocks, in close spatial association with granitoids having quartz and quartzofeldspathic veins representing hydrothermal activities associated with them. Mineralized quartz veins from the ore zones (in Ramagiri and Penakacherla regions) and quartz (or pegmatitic) veins from the surrounding granitic terrane were chosen for δ18O analysis. Samples from the schistose and granitic domains show δ18Oquartz values in the range of 10.4–14.9 and 9.3–10.9‰ respectively. The ore-zone fluids from the Ramagiri and Penakacherla regions give δ18O values of 7.9 ± 1.5 and 5.1 ± 0.8‰, calculated at pressure-corrected temperatures obtained from fluid inclusion microthermometry. The late-magmatic fluid is relatively 18O-poor with δ18O values estimated at 4.5 ± 0.7‰ and the value is closer to what is obtained for the ore zones. Based on the δ18O values reported and a possible magmatic contribution to ore fluid deciphered from fluid inclusion characteristics, a genetic relationship between granitic magmatism and gold mineralization is surmised. The observed increase in the 18O/16O ratio from the magmatic fluid to ore fluid in the shear zone is attributed to interaction of the magmatic fluid with host metasediments, that agrees well with the variation in the CO2/CH4 ratio of carbonic component in such fluids.  相似文献   

20.
《Quaternary Science Reviews》1999,18(8-9):1021-1038
Time-series O isotope profiles for three U–Th dated stalagmites have revealed that for much of the Holocene, a site on the Atlantic seaboard (SW Ireland) exhibits first-order δ18O trends that are almost exactly out of phase with coupled δ18O curves from two southern European sites (SE France and NW Italy). In the Irish stalagmite (CC3 from Crag Cave, SW Ireland), low δ18O at 10,000 cal yr BP reflects cool conditions. By the early to mid-Holocene (9000–6000 cal yr BP) δ18O had increased, reflecting the onset of warmer conditions on the Atlantic seaboard. This shift to higher δ18O was accompanied by a marked increase in the stalagmite extension rate, reinforcing our interpretation that this was a period of relative warmth. Except for an episode of increased extension rate about 5500 yr ago, δ18O in the Crag stalagmite exhibits a gradual decrease, accompanied by declining extension rates between 7800 and 3500 cal yr BP, interpreted as a cooling trend. There is evidence for increases in both δ18O and stalagmite extension rate in the period from 3500 cal yr BP to the present day suggesting a return to warmer conditions on the Atlantic seaboard. In the stalagmite from NW Italy (ER76, Grotta di Ernesto, Trentino province) the early-Holocene (c. 9200-7800 cal yr BP) is characterised by high δ18O, probably indicative of warm and/or dry conditions. Exceptionally low δ18O from 7800 to 6900 cal yr BP at this site reflects a well-defined wet phase (Cerin wet phase). In the last three millennia, this stalagmite exhibits a shift to lower δ18O, interpreted as some combination of cooler and/or wetter conditions. Unlike the Irish stalagmite, the Italian sample does not show a correlation between δ18O and extension rate. Instead, its extension rate correlates roughly with δ13C, presumably reflecting a climate-driven vegetation change. In the early Holocene, δ18O in the French stalagmite (CL26, Grotte de Clamouse, Herault province, SE France) was low relative to its Holocene average. For much of the period since c. 3500 cal yr BP this stalagmite exhibits higher δ18O than in the early Holocene, suggesting warmer conditions. Like the Irish stalagmite, the French sample exhibits a well-defined correlation between δ18O and extension rate. Had drip-water availability been the dominant control on δ18O at this semi-arid site then higher δ18O would have been accompanied by lower, not higher extension rates. This suggests strongly that temperature rather than rainfall amount was the dominant control at this site. While conclusions regarding the patterns of climate variability on a continent scale must remain tentative because of the limited number of stalagmites studied we argue that early Holocene warm conditions on the Atlantic seaboard (Irish site) coincided with relatively cool conditions at the Clamouse site. By c. 3500 yr ago the pattern appears to have been reversed.  相似文献   

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